Clinical Trial

Postpartum Evaluation of Nifedipine and Enalapril for Hypertension

Study acronym: PEACE
Recruiting Phase 4
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Summary
This is an open label, randomized controlled trial designed to compare nifedipine and enalapril in the management of postpartum hypertension. This is an equivalence study- meaning it is not expected one medication is better than the other. Nifedipine has been shown to be better than another common blood pressure medicine, labetalol, for postpartum hypertension but enalapril which is also used worldwide to manage blood pressure postpartum, has not yet been evaluated or compared to nifedipine. Investigators will identify and offer enrollment to women who are admitted for delivery with documented hypertension- participants with either chronic hypertension or pregnancy related hypertension will be included. Our hypothesis is both medications are safe and effective in managing blood pressure and preventing readmission for hypertensive complications during the postpartum period so evaluating the rate of readmission is the primary goal of the study. The only intervention of the trial will be to assign which medication the participant starts taking. Any decisions after that point- stopping medication, changing doses, additional medications, discharge from the hospital, etc, will all be at the discretion of the participant's primary provider.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-06-08; most recent amendment 2025-10-20.
Status change: Not Yet Recruiting → Recruiting 2025-10-20
Trial Details
NCT Number NCT07023003
Lead Sponsor Nebraska Methodist Health System
Collaborators: Methodist Hospital Foundation
Conditions Hypertension in Pregnancy
Enrollment 850 participants
Start Date 2025-07-11
Primary Completion 2028-07 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2025-10-22